Catalog No.:AA003SR4

73365-02-3 | N-(tert-Butoxycarbonyl)-D-prolinal

Name: Name:N-(tert-Butoxycarbonyl)-D-prolinal
Brand: AABLOCKS
SKU: AA003SR4
Availability: InStock
Rating: 90 (10 reviews)

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Price(USD)

Quantity

97%

in stock

$16.00 $11.00

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97%

in stock

$19.00 $14.00

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10g

97%

in stock

$37.00 $26.00

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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
Request for Quotation
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003SR4

Chemical Name:

N-(tert-Butoxycarbonyl)-D-prolinal

CAS Number:

73365-02-3

Molecular Formula:

C10H17NO3

Molecular Weight:

199.2469

MDL Number:

MFCD01321389

SMILES:

O=C[C@H]1CCCN1C(=O)OC(C)(C)C

Properties

BP:

276.3°C at 760 mmHg

Form:

Liquid

Refractive Index:

n20/D 1.461(lit.)

Stability:

Air Sensitive

Storage:

Inert atmosphere;-20 ℃;

Computed Properties

Complexity:

232

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

XLogP3:

1.2

Upstream Synthesis Route

59378-81-3

73365-02-3

[1]Patent:WO2015/120390,2015,A1,.Locationinpatent:Page/Pagecolumn97;178

[2]TetrahedronLetters,1997,vol.38,#37,p.6479-6482

[3]Patent:WO2015/118342,2015,A1,.Locationinpatent:Page/Pagecolumn94;95

[4]JournalofMedicinalChemistry,1990,vol.33,#12,p.3190-3198

[5]TetrahedronLetters,1990,vol.31,#28,p.3957-3960

[6]JournalofMedicinalChemistry,1992,vol.35,#9,p.1550-1557

[7]JournalofMedicinalChemistry,1994,vol.37,#4,p.439-445

[8]EuropeanJournalofOrganicChemistry,1998,#6,p.945-959

[9]OrganicLetters,2009,vol.11,#12,p.2491-2494

[10]Patent:EP1553074,2005,A1,.Locationinpatent:Page/Pagecolumn49-50

[11]Patent:US2010/160352,2010,A1,.Locationinpatent:Page/Pagecolumn16

[12]BioorganicandMedicinalChemistry,2010,vol.18,#7,p.2720-2727

[13]Patent:US2011/263561,2011,A1,.Locationinpatent:Page/Pagecolumn20-21

[14]Nature,2014,vol.509,#7500,p.318-324

[15]RSCAdvances,2016,vol.6,#31,p.25713-25723

[16]Patent:CN108314639,2018,A,.Locationinpatent:Paragraph0069;0070;0071

852324-75-5

73365-02-3

[1]Patent:WO2005/47253,2005,A1,.Locationinpatent:Page/Pagecolumn46

37784-17-1

73365-02-3

[1]OrganicLetters,2006,vol.8,#23,p.5357-5360

[2]EuropeanJournalofMedicinalChemistry,2000,vol.35,#11,p.979-988

[3]JournalofMedicinalChemistry,1992,vol.35,#9,p.1550-1557

[4]JournalofMedicinalChemistry,1990,vol.33,#12,p.3190-3198

[5]TetrahedronLetters,1990,vol.31,#28,p.3957-3960

[6]Patent:US2011/263561,2011,A1,

[7]Nature,2014,vol.509,#7500,p.318-324

[8]RSCAdvances,2016,vol.6,#31,p.25713-25723

[9]Patent:WO2017/21728,2017,A1,.Locationinpatent:Page/Pagecolumn53

201230-82-2

73286-71-2

69610-41-9

73365-02-3

[1]JournalofOrganicChemistry,1980,vol.45,#11,p.2145-2151

79-37-8

59378-81-3

73365-02-3

[1]Patent:US5620959,1997,A,

Downstream Synthesis Route

3610-42-2

73365-02-3

147292-60-2

[1]ArchivderPharmazie,1993,vol.326,p.33-37

75-11-6

73365-02-3

340129-94-4

[1]ChemistryLetters,1987,p.2085-2088

558-13-4

73365-02-3

130418-88-1

[1]JournalofMedicinalChemistry,1990,vol.33,p.3190-3198

[2]TetrahedronLetters,1990,vol.31,p.3957-3960

[3]JournalofMedicinalChemistry,1992,vol.35,p.1550-1557

[4]Patent:WO2005/103020,2005,A1.Locationinpatent:Page/Pagecolumn87-88

[5]Patent:WO2019/94143,2019,A1.Locationinpatent:Paragraph174

2577-90-4

73365-02-3

(R)-2-(E)-(S)-1-Methoxycarbonyl-2-phenyl-ethylimino-methyl}-pyrrolidine-1-carboxylicacidtert-butylester

[1]JournalofMedicinalChemistry,1994,vol.37,p.439-445

73365-02-3

261900-93-0

(R)-2-(S)-1-Hydroxy-3-((R)-toluene-4-sulfinyl)-but-3-enyl-pyrrolidine-1-carboxylicacidtert-butylester

399559-57-0

[1]JournalofOrganicChemistry,2002,vol.67,p.308-311

Literature

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